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FDA 510(k)

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS

K-Number: K901997 · 1990-06-06

ApplicantComet Ltd. C/O Radiology Resources, Inc.
Decision Date1990-06-06
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Comet Ltd. C/O Radiology Resources, Inc.. It received FDA 510(k) clearance on 1990-06-06 under 510(k) number K901997. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS?

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1990-06-06. The listed applicant is Comet Ltd. C/O Radiology Resources, Inc.. The 510(k) number is K901997.

When did X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS receive FDA 510(k) clearance?

X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS received FDA 510(k) clearance on 1990-06-06, under 510(k) number K901997.

Who is the listed applicant for X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS?

The FDA 510(k) record lists Comet Ltd. C/O Radiology Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS?

The FDA product code for X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS is IZH.

Related Clinical Trials

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Other records listing Comet Ltd. C/O Radiology Resources, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K912338TUBE HOUSING ASSEMBLIESK911695VARIOUS X-RAY TUBESK910842DI2000/HS-45-150 X-RAY TUBE INSERTK864749TELAMAT

Related Devices (Code: IZH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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